FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MODEL 2100 MILD INTERMITTENT SUCTION PUMP
K Number: K941524
·
Decision May 17, 1994
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
76
Applicant Total
4
Review Days
48
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Basic Information
- Device Name
- MODEL 2100 MILD INTERMITTENT SUCTION PUMP
- K Number
- K941524
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.4780
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Product & Educational Services
- Date Received
- March 30, 1994
- Decision Date
- May 17, 1994
- Product Code
- JCX
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| JCX | Apparatus, Suction, Ward Use, Portable, Ac-Powered | FDA class 2 | General, Plastic Surgery |
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